HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337655Generated: October 30, 2026
Diisobutylaluminum hydride → 3-Bromo-5-[3-(difluoromethoxy)propyl]-4-methylbenzaldehyde
https://huagongshe.com/reaction/337655
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 3-bromo-5-[3-(difluoromethoxy)propyl]-4-methylbenzoate | HCID 66896426 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-5-[3-(difluoromethoxy)propyl]-4-methylbenzaldehyde | HCID 87195351 | — |
Reaction Steps
To a dichloromethane (0.07 M) solution of methyl 3-bromo-5-[3-(difluoromethoxy)propyl]-4-methylbenzoate (1 eq.) from the previous step was added DIBAL-H (1.5 M solution in toluene, 2.2 eq.). The resulting solution was stirred at RT for 1.5 h and then carefully quenched with 10% aq. HCl. The aqueous layer was separated and back-extracted with ether. The combined organic extracts were washed further with brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. The crude alcohol thus obtained was taken up again in dichloromethane (0.07 M) and then added Dess-Martin periodinane (1.0 eq.) and sodium bicarbonate (1.2 eq.). After stirring at RT for 40 min, the reaction mixture was diluted with ether and washed sequentially with sat. aq. NaHSO3, 1 N aq. NaOH, water and brine. The organic extract was dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Purification of the crude product by way of flash chromatography (SiO2, Hex→1:1 (v/v) Hex:EtOAc) afforded the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889714B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-543543beb3dc4805b702c10491aef241 |
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| Source note | uspto-grants-2014_11 |
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